Lazega D, Schenker E, Busso N, Zelent A, Chen A, Waxman S
Division of Medical Oncology, Mount Sinai School of Medicine, New York, New York 10029.
J Cell Physiol. 1993 Oct;157(1):90-6. doi: 10.1002/jcp.1041570112.
F9 embryonal carcinoma cells differentiate in response to retinoic acid (RA). To investigate the regulation of RA receptors (RARs) expression during this process, cDNA probes specific for the major RAR isoforms were used. In contrast to the level of RAR beta 2 mRNA which was high in cells treated 5 days with RA and below detection in untreated cells, as previously described, the steady state levels of RAR alpha 1, alpha 2, gamma 1, and gamma 2 mRNAs were markedly decreased in the RA-differentiated cells as compared to untreated cells. The down-regulation of the RA-responsive system in differentiated cells was also evident in gel shift assays as a marked decrease in binding capacity to a retinoid acid response element (beta 2RARE), as well as in chloramphenicol acetyltransferase (CAT) assays as a sixfold decrease in RA-mediated transacting activity via this element. The down-regulation of RAR DNA-binding and transacting activity coincided with the burst in tissue plasminogen activator secretion and thus, occurred at the hinge between early and late differentiation. The down-regulation of RA responsiveness may constitute an important event in the transition between early and late differentiation stage in F9 cells.
F9胚胎癌细胞会因视黄酸(RA)而发生分化。为了研究在此过程中视黄酸受体(RARs)表达的调控情况,使用了针对主要RAR亚型的cDNA探针。与之前所描述的情况一样,在用RA处理5天的细胞中RARβ2 mRNA水平较高,而在未处理的细胞中低于检测水平,与之相反,与未处理的细胞相比,RA分化细胞中RARα1、α2、γ1和γ2 mRNA的稳态水平显著降低。在凝胶迁移试验中,分化细胞中RA反应系统的下调也很明显,表现为与视黄酸反应元件(β2RARE)的结合能力显著下降,在氯霉素乙酰转移酶(CAT)试验中,通过该元件的RA介导的反式作用活性下降了六倍。RAR DNA结合和反式作用活性的下调与组织纤溶酶原激活物分泌的激增同时发生,因此,发生在早期和晚期分化的衔接点。RA反应性的下调可能是F9细胞早期和晚期分化阶段转变中的一个重要事件。